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2,2,5,7,8-Pentamethylchroman-6-sulfonyl chloride is a chemical compound with the molecular formula C15H21ClO3S. It is a sulfonyl chloride derivative of pentamethylchroman, an organic compound known for its antioxidant properties. This specific compound is characterized by its highly reactive and versatile nature, making it a valuable reagent in organic synthesis for the preparation of various other organic compounds.

112160-39-1

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112160-39-1 Usage

Uses

Used in Organic Synthesis:
2,2,5,7,8-Pentamethylchroman-6-sulfonyl chloride is used as a reagent in organic synthesis for the preparation of various other organic compounds. Its sulfonyl chloride group makes it a valuable tool in the formation of carbon-carbon and carbon-heteroatom bonds, contributing to the synthesis of complex organic molecules.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 2,2,5,7,8-Pentamethylchroman-6-sulfonyl chloride is used as a key intermediate in the synthesis of various pharmaceuticals. Its antioxidant properties and reactivity in organic synthesis make it a useful building block for the development of new drugs with potential therapeutic applications.
Used in Agrochemical Industry:
2,2,5,7,8-Pentamethylchroman-6-sulfonyl chloride is also used in the agrochemical industry as a precursor for the synthesis of various agrochemicals. Its versatility in organic synthesis allows for the development of new compounds with potential applications in crop protection and other agricultural areas.
Used in Specialty Chemicals Production:
2,2,5,7,8-Pentamethylchroman-6-sulfonyl chloride is used as a reagent in the production of specialty chemicals. Its unique properties and reactivity make it a valuable component in the synthesis of high-value specialty chemicals for various applications, including materials science, coatings, and other industrial processes.

Check Digit Verification of cas no

The CAS Registry Mumber 112160-39-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,2,1,6 and 0 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 112160-39:
(8*1)+(7*1)+(6*2)+(5*1)+(4*6)+(3*0)+(2*3)+(1*9)=71
71 % 10 = 1
So 112160-39-1 is a valid CAS Registry Number.
InChI:InChI=1/C14H19ClO3S/c1-8-9(2)13(19(15,16)17)10(3)11-6-7-14(4,5)18-12(8)11/h6-7H2,1-5H3

112160-39-1 Well-known Company Product Price

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  • Aldrich

  • (25649)  2,2,5,7,8-Pentamethyl-chromane-6-sulfonylchloride  ≥97.0% (HPLC)

  • 112160-39-1

  • 25649-1G

  • 1,969.11CNY

  • Detail
  • Aldrich

  • (25649)  2,2,5,7,8-Pentamethyl-chromane-6-sulfonylchloride  ≥97.0% (HPLC)

  • 112160-39-1

  • 25649-5G

  • 6,522.75CNY

  • Detail

112160-39-1SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,2,5,7,8-pentamethyl-3,4-dihydrochromene-6-sulfonyl chloride

1.2 Other means of identification

Product number -
Other names 2,2,5,7,8-Pentamethyl-chromane-6-sulfonyl chloride

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:112160-39-1 SDS

112160-39-1Relevant articles and documents

Enantioselective total synthesis of (-)-dehydrobatzelladine C

Collins, Shawn K.,McDonald, Andrew I.,Overman, Larry E.,Rhee, Young Ho

, p. 1253 - 1255 (2004)

The oxidation of two tethered Biginelli adducts was examined as a potential key step in total syntheses of highly oxidized batzelladine and crambescidin alkaloids. Although angular hydroxyl substitution could not be introduced, dehydrogenation was readily accomplished. This latter conversion is a key step in the first total synthesis of dehydrobatzelladine C.

Inhibition of tumor growth

-

, (2015/09/22)

The present invention provides a cytotoxic 7 to 25 mer peptide with three or more cationic residues which has one or more non-genetic bulky and lipophilic amino acids, as well as esters, amides, salts and cyclic derivatives thereof as well as methods of p

Bioactive peptides

-

, (2008/06/13)

The present invention provides a modified lactoferrin peptide which is cytotoxic, 7 to 25 amino acids in length, with three or more cationic residues and which has one or more extra bulky and lipophilic amino acids as compared to the native lactoferrin sequence, as well as esters, amides, salts and cyclic derivatives thereof as well as methods of preparing such peptides, pharmaceutical compositions containing such peptides and use of the peptides as medicaments, particularly as antibacterials or anti-tumoural agents.

An acid labile arginine derivative for peptide synthesis: N(G)-2,2,5,7,8-pentamethylchroman-6-sulphonyl-L-arginine

Ramage,Green,Blake

, p. 6353 - 6370 (2007/10/02)

A trifluoroacetic acid (TFA) labile protecting group for the guanidine side chain function of arginine has been developed. N(G)-(2,2,5,7,8-Pentamethylchroman-6-sulphonyl-L-arginine is cleaved rapidly in TFA or 50% TFA in dichloromethane at room temperatur

NG-2,2,5,7,8-PENTAMETHYLCHROMAN-6-SULPHONYL-L-ARGININE: A NEW ACID LABILE DERIVATIVE FOR PEPTIDE SYNTHESIS

Ramage, R.,Green, J.

, p. 2287 - 2290 (2007/10/02)

A new acid labile protecting group for the guanido side chain functionality of arginine has been developed.NG-(2,2,5,7,8-Pentamethylchroman-6-sulphonyl)-L-arginine, prepared from Nα-benzyloxycarbonyl-L-arginine and 2,2,5,7,8-pentamethylchroman-6-sulphonyl chloride, is cleaved rapidly in trifluoroacetic acid (TFA) or 50percent TFA in dichloromethane at room temperature.

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